chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	126894919	126894920	C	T	24	GENIC	possibly homozygous	114441096
5	126895049	126895050	A	G	43	GENIC	possibly homozygous	114137517
5	126895299	126895300	T	C	24	GENIC	homozygous	114137519
5	126895554	126895555	A	G	25	GENIC	homozygous	114441098
5	126895611	126895612	C	T	37	GENIC	homozygous	114137520
5	126895649	126895650	C	T	38	GENIC	homozygous	114441100
5	126895672	126895673	G	C	37	GENIC	homozygous	114441102
5	126896500	126896501	T	C	30	GENIC	homozygous	113999404
5	126896521	126896522	T	C	28	GENIC	homozygous	113999406
5	126897154	126897155	C	T	27	GENIC	homozygous	114441104
5	126897157	126897158	C	A	27	GENIC	homozygous	113999410
5	126897845	126897846	A	G	21	GENIC	homozygous	113999412
5	126897879	126897880	T	C	38	GENIC	heterozygous	114441106
5	126897943	126897944	T	C	40	GENIC	homozygous	113999420
5	126899585	126899586	C	T	37	GENIC	homozygous	114441108
5	126899951	126899952	C	G	35	GENIC	homozygous	113999428
5	126900226	126900227	G	A	19	GENIC	homozygous	113999432
5	126900301	126900302	C	T	9	GENIC	heterozygous	113999434
5	126900665	126900666	T	A	34	GENIC	possibly homozygous	114441110
5	126900937	126900938	G	T	41	GENIC	homozygous	114441112
5	126905458	126905459	T	C	27	GENIC	homozygous	113999458
5	126905810	126905811	A	G	61	GENIC	heterozygous	113999460
5	126906071	126906072	A	G	25	GENIC	homozygous	113999474
5	126907319	126907320	C	G	52	GENIC	heterozygous	114137531
5	126907721	126907722	C	T	18	GENIC	homozygous	114441114
5	126907907	126907908	G	A	30	GENIC	homozygous	114441116
5	126908245	126908246	G	A	32	GENIC	homozygous	113999496
5	126908401	126908402	C	T	55	GENIC	heterozygous	113999500
5	126910989	126910990	A	G	39	GENIC	homozygous	114441118